Endo USA recalls 2mg Clonazepam orally disintegrating tablets with incorrect labeling. Some cartons show wrong strength but blister strips are correct. No action needed as the tablets are safe to use.
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength.
Endo USA is recalling 2mg Clonazepam orally disintegrating tablets due to a labeling error in some cartons. The error means the label shows the wrong strength, but the actual tablets inside are correct. This does not pose a safety risk to users.
The product carton label shows an incorrect strength, but the blister strips inside the carton correctly indicate the 2mg strength. This labeling error does not affect the actual medication content or safety.
Prescription users of Endo's 2mg Clonazepam orally disintegrating tablets who received the recalled cartons with incorrect labeling. Those most at risk are individuals using the medication as directed without noticing the label error.
Check for cartons labeled with NDC 49884-310-02 (carton) or 49884-310-52 (blisters) from Endo USA. The product was distributed with lot numbers 550176501 or 550176601 and expires February 28, 2027.
Verify the blister strip inside the carton shows the correct 2mg strength. The carton label may show an incorrect strength.
No, the labeling error does not affect the medication's safety. The tablets are correctly dosed inside the blister strips.
No action is needed. The tablets are safe to use as directed since the blister strips show the correct strength.
Check for cartons with NDC 49884-310-02 (carton) or 49884-310-52 (blisters) and lot numbers 550176501 or 550176601.
We’ve drafted a message you can send Endo to request your refund or repair — edit it as you like.
Subject: Recall D-0178-2025 — Endo Endo Hello, I own a Endo that is covered by recall D-0178-2025 from Endo. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
